gudid Primary ID: 0009-00

Innomed, Inc. (UDI 0009-00)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Innomed, Inc. (Model/Catalog Number: 0009-00) is a medical device manufactured by INNOMED, INC.. This product is indexed under FDA Product Code / Category Classification KIL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0009-00
Product Code / EMDN: KIL
Device Name: Jackson Ankle Distraction Set
Database Sync Date: 2026-08-09 09:12:06

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Innomed, Inc.?

The registered manufacturer of record for Innomed, Inc. is INNOMED, INC..

What is the Primary UDI-DI identifier for Innomed, Inc.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0009-00.

What classification code is assigned to this device?

This device is registered under product classification code KIL.

Similar Classification Devices (KIL)

Other Devices by INNOMED, INC.

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